Variant report

Variant	rs4237489
Chromosome Location	chr10:117626075-117626076
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1552068	0.92[YRI][hapmap];0.94[AFR][1000 genomes]
rs17093691	1.00[AMR][1000 genomes]
rs2620952	0.81[YRI][hapmap];0.93[AFR][1000 genomes]
rs2620953	0.92[YRI][hapmap];0.93[AFR][1000 genomes]
rs2960658	0.98[AFR][1000 genomes]
rs4328148	0.92[YRI][hapmap];0.94[AFR][1000 genomes]
rs4751570	0.93[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4751934	0.81[AFR][1000 genomes]
rs7922443	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117612200-117628000	Weak transcription	Ovary	ovary
2	chr10:117625200-117627200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr10:117625400-117626400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:117626000-117626400	Enhancers	Fetal Brain Female	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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